Статті в журналах з теми "Alkynoate"
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Zeng, Yao-Fu, Dong-Hang Tan, Yunyun Chen, Wen-Xin Lv, Xu-Ge Liu, Qingjiang Li, and Honggen Wang. "Direct radical trifluoromethylthiolation and thiocyanation of aryl alkynoate esters: mild and facile synthesis of 3-trifluoromethylthiolated and 3-thiocyanated coumarins." Organic Chemistry Frontiers 2, no. 11 (2015): 1511–15. http://dx.doi.org/10.1039/c5qo00271k.
Повний текст джерелаAparece, Mark D., and Paul A. Vadola. "Gold-Catalyzed Dearomative Spirocyclization of Aryl Alkynoate Esters." Organic Letters 16, no. 22 (November 3, 2014): 6008–11. http://dx.doi.org/10.1021/ol503022h.
Повний текст джерелаSong, Zefeng, Weijia Wang, Zhixin Liu, Yue Lu, and De Wang. "Phosphine-Catalyzed Intermolecular Dienylation of Alkynoate with para-Quinone Methides." Journal of Organic Chemistry 86, no. 13 (June 24, 2021): 8590–99. http://dx.doi.org/10.1021/acs.joc.1c00226.
Повний текст джерелаValette, Damien, Yajing Lian, John P. Haydek, Kenneth I. Hardcastle, and Huw M. L. Davies. "Alkynoate Synthesis through the Vinylogous Reactivity of Rhodium(II) Carbenoids." Angewandte Chemie 124, no. 34 (July 16, 2012): 8764–67. http://dx.doi.org/10.1002/ange.201204047.
Повний текст джерелаAparece, Mark D., and Paul A. Vadola. "ChemInform Abstract: Gold-Catalyzed Dearomative Spirocyclization of Aryl Alkynoate Esters." ChemInform 46, no. 18 (April 16, 2015): no. http://dx.doi.org/10.1002/chin.201518113.
Повний текст джерелаValette, Damien, Yajing Lian, John P. Haydek, Kenneth I. Hardcastle, and Huw M. L. Davies. "Alkynoate Synthesis through the Vinylogous Reactivity of Rhodium(II) Carbenoids." Angewandte Chemie International Edition 51, no. 34 (July 16, 2012): 8636–39. http://dx.doi.org/10.1002/anie.201204047.
Повний текст джерелаImagawa, Hiroshi, Atsushi Kinoshita, Takashi Fukuyama, Hirofumi Yamamoto, and Mugio Nishizawa. "Hg(OTf)2-catalyzed glycosylation using alkynoate as the leaving group." Tetrahedron Letters 47, no. 27 (July 2006): 4729–31. http://dx.doi.org/10.1016/j.tetlet.2006.04.114.
Повний текст джерелаSchäfer, Christian, Michel Miesch та Laurence Miesch. "Intramolecular reductive ketone–alkynoate coupling reaction promoted by (η2-propene)titanium". Organic & Biomolecular Chemistry 10, № 16 (2012): 3253. http://dx.doi.org/10.1039/c2ob07049a.
Повний текст джерелаValette, Damien, Yajing Lian, John P. Haydek, Kenneth I. Hardcastle, and Huw M. L. Davies. "ChemInform Abstract: Alkynoate Synthesis Through the Vinylogous Reactivity of Rhodium(II) Carbenoids." ChemInform 44, no. 3 (January 15, 2013): no. http://dx.doi.org/10.1002/chin.201303045.
Повний текст джерелаSchaefer, Christian, Michel Miesch та Laurence Miesch. "ChemInform Abstract: Intramolecular Reductive Ketone-Alkynoate Coupling Reaction Promoted by (η2-Propene)titanium." ChemInform 43, № 38 (23 серпня 2012): no. http://dx.doi.org/10.1002/chin.201238029.
Повний текст джерелаBrecker, Lothar, Julia Petschnigg, Nicole Depine, Hansjorg Weber, and Douglas W. Ribbons. "In situ proton NMR analysis of alpha-alkynoate biotransformations. From 'invisible' substrates to detectable metabolites." European Journal of Biochemistry 270, no. 7 (April 2003): 1393–98. http://dx.doi.org/10.1046/j.1432-1033.2003.03460.x.
Повний текст джерелаSong, Bo, Rongyuan Zhang, Rong Hu, Xu Chen, Dongming Liu, Jiali Guo, Xiaotian Xu, Anjun Qin, and Ben Zhong Tang. "Site‐Selective, Multistep Functionalizations of CO 2 ‐Based Hyperbranched Poly(alkynoate)s toward Functional Polymetric Materials." Advanced Science 7, no. 17 (July 8, 2020): 2000465. http://dx.doi.org/10.1002/advs.202000465.
Повний текст джерелаZhang, Jiayong, Cheng Cheng, Dian Wang, and Zhiwei Miao. "Regio- and Diastereoselective Construction of Spirocyclopenteneoxindoles through Phosphine-Catalyzed [3 + 2] Annulation of Methyleneindolinone with Alkynoate Derivatives." Journal of Organic Chemistry 82, no. 19 (September 21, 2017): 10121–28. http://dx.doi.org/10.1021/acs.joc.7b01582.
Повний текст джерелаLuo, Zaigang, Yuyu Fang, Yu Zhao, Peng Liu, Xuemei Xu, Chengtao Feng, Zhong Li, and Jie He. "Synthesis of multisubstituted furans via Cu(i)-catalyzed annulation of ketones with alkynoate under ligand- and additive-free conditions." RSC Advances 6, no. 7 (2016): 5436–41. http://dx.doi.org/10.1039/c5ra23058f.
Повний текст джерелаKamijo, Shin, Kaori Kamijo, Daiki Magarifuchi, Ryota Ozawa, Keisuke Tao, and Toshihiro Murafuji. "Two-directional carbon chain elongation via the consecutive 1,4-addition of allyl malononitrile and the Cope rearrangement on an alkynoate platform." Tetrahedron Letters 57, no. 1 (January 2016): 137–40. http://dx.doi.org/10.1016/j.tetlet.2015.11.081.
Повний текст джерелаZeng, Yao-Fu, Dong-Hang Tan, Yunyun Chen, Wen-Xin Lv, Xu-Ge Liu, Qingjiang Li, and Honggen Wang. "ChemInform Abstract: Direct Radical Trifluoromethylthiolation and Thiocyanation of Aryl Alkynoate Esters: Mild and Facile Synthesis of 3-Trifluoromethylthiolated and 3-Thiocyanated Coumarins." ChemInform 47, no. 13 (March 2016): no. http://dx.doi.org/10.1002/chin.201613151.
Повний текст джерелаChe, Jiuwei, Alavala Gopi Krishna Reddy, Li Niu, Dong Xing та Wenhao Hu. "Cu(I)-Catalyzed Three-Component Reaction of α-Diazo Amide with Terminal Alkyne and Isatin Ketimine via Electrophilic Trapping of Active Alkynoate-Copper Intermediate". Organic Letters 21, № 12 (3 червня 2019): 4571–74. http://dx.doi.org/10.1021/acs.orglett.9b01470.
Повний текст джерелаZhu, Mei, Weijun Fu, Zhiqiang Wang, Chen Xu, and Baoming Ji. "Visible-light-mediated direct difluoromethylation of alkynoates: synthesis of 3-difluoromethylated coumarins." Organic & Biomolecular Chemistry 15, no. 43 (2017): 9057–60. http://dx.doi.org/10.1039/c7ob02366a.
Повний текст джерелаZhang, Wei, Chen Yang, Yu-Liang Pan, Xin Li, and Jin-Pei Cheng. "Synthesis of 3-cyanomethylated coumarins by a visible-light-mediated direct cyanomethylation of aryl alkynoates." Organic & Biomolecular Chemistry 16, no. 32 (2018): 5788–92. http://dx.doi.org/10.1039/c8ob01513a.
Повний текст джерелаKong, Hongjun, Qingrui Li, Yunnian Yin, Mengmeng Huang, Jung Keun Kim, Yu Zhu, Yabo Li, and Yangjie Wu. "An efficient light on–off one-pot method for the synthesis of 3-styryl coumarins from aryl alkynoates." Organic & Biomolecular Chemistry 17, no. 18 (2019): 4621–28. http://dx.doi.org/10.1039/c9ob00421a.
Повний текст джерелаLi, Huan, Shuai Liu, Yangen Huang, Xiu-Hua Xu, and Feng-Ling Qing. "Tandem trifluoromethylthiolation/aryl migration of aryl alkynoates to trifluoromethylthiolated alkenes." Chemical Communications 53, no. 73 (2017): 10136–39. http://dx.doi.org/10.1039/c7cc06232j.
Повний текст джерелаDavey, Stephen. "Addition to alkynoates." Nature Chemistry 6, no. 9 (August 21, 2014): 754. http://dx.doi.org/10.1038/nchem.2051.
Повний текст джерелаLi, Qingrui, Yunnian Yin, Yabo Li, Jianye Zhang, Mengmeng Huang, Jung Keun Kim, and Yangjie Wu. "A simple approach to indeno-coumarins via visible-light-induced cyclization of aryl alkynoates with diethyl bromomalonate." Organic Chemistry Frontiers 6, no. 18 (2019): 3238–43. http://dx.doi.org/10.1039/c9qo00795d.
Повний текст джерелаKhan, Imtiaz, Sumera Zaib, and Aliya Ibrar. "New frontiers in the transition-metal-free synthesis of heterocycles from alkynoates: an overview and current status." Organic Chemistry Frontiers 7, no. 22 (2020): 3734–91. http://dx.doi.org/10.1039/d0qo00698j.
Повний текст джерелаKong, De-Long, Liang Cheng, Hong-Ru Wu, Yang-Xiong Li, Dong Wang, and Li Liu. "A metal-free yne-addition/1,4-aryl migration/decarboxylation cascade reaction of alkynoates with Csp3–H centers." Organic & Biomolecular Chemistry 14, no. 7 (2016): 2210–17. http://dx.doi.org/10.1039/c5ob02478a.
Повний текст джерелаFeng, Shangbiao, Jinlai Li, Zaimin Liu, Haiyu Sun, Hongliang Shi, Xiaolei Wang, Xingang Xie, and Xuegong She. "Visible-light-mediated radical cascade reaction: synthesis of 3-bromocoumarins from alkynoates." Org. Biomol. Chem. 15, no. 41 (2017): 8820–26. http://dx.doi.org/10.1039/c7ob02199b.
Повний текст джерелаLi, Zun, Jia Zheng, Weigao Hu, Jianxiao Li, Wanqing Wu, and Huanfeng Jiang. "Synthesis of 1,4-enyne-3-ones via palladium-catalyzed sequential decarboxylation and carbonylation of allyl alkynoates." Organic Chemistry Frontiers 4, no. 7 (2017): 1363–66. http://dx.doi.org/10.1039/c7qo00082k.
Повний текст джерелаWang, Qiumei, Chao Yang, and Chao Jiang. "Visible-light-promoted radical acylation/cyclization of alkynoates with aldehydes for the synthesis of 3-acylcoumarins." Organic & Biomolecular Chemistry 16, no. 43 (2018): 8196–204. http://dx.doi.org/10.1039/c8ob02232a.
Повний текст джерелаPan, Changduo, Rongzhen Chen, Weile Shao та Jin-Tao Yu. "Metal-free radical addition/cyclization of alkynoates with xanthates towards 3-(β-carbonyl)coumarins". Organic & Biomolecular Chemistry 14, № 38 (2016): 9033–39. http://dx.doi.org/10.1039/c6ob01732k.
Повний текст джерелаChen, Pu, Zan Chen, Bi-Quan Xiong, Yun Liang, Ke-Wen Tang, Jun Xie, and Yu Liu. "Visible-light-mediated cascade cyanoalkylsulfonylation/cyclization of alkynoates leading to coumarins via SO2 insertion." Organic & Biomolecular Chemistry 19, no. 14 (2021): 3181–90. http://dx.doi.org/10.1039/d1ob00142f.
Повний текст джерелаChen, Yan-Shan, Yu Zheng, Zhi-Jun Chen, Zhen-Zhen Xie, Xian-Chen He, Jun-An Xiao, Kai Chen, Hao-Yue Xiang, and Hua Yang. "A phosphine-catalysed one-pot domino sequence to access cyclopentene-fused coumarins." Organic & Biomolecular Chemistry 19, no. 32 (2021): 7074–80. http://dx.doi.org/10.1039/d1ob01143j.
Повний текст джерелаWei, Wei, Leilei Wang, Huilan Yue, Yuan-Ye Jiang та Daoshan Yang. "Catalyst-free synthesis of α-thioacrylic acids via cascade thiolation and 1,4-aryl migration of aryl alkynoates at room temperature". Organic & Biomolecular Chemistry 16, № 37 (2018): 8379–83. http://dx.doi.org/10.1039/c8ob01349g.
Повний текст джерелаHeinrich, Clément F., Michel Miesch, and Laurence Miesch. "In situ intramolecular catalytic 1,2-addition of allenoates to cyclic ketones towards polycyclic allenoates." Organic & Biomolecular Chemistry 13, no. 7 (2015): 2153–56. http://dx.doi.org/10.1039/c4ob02451f.
Повний текст джерелаEşsiz, Selçuk. "A computational study for the reaction mechanism of metal-free cyanomethylation of aryl alkynoates with acetonitrile." RSC Advances 11, no. 30 (2021): 18246–51. http://dx.doi.org/10.1039/d1ra01649k.
Повний текст джерелаSau, Sudip, and Prasenjit Mal. "3-Nitro-coumarin synthesis via nitrative cyclization of aryl alkynoates using tert-butyl nitrite." Chemical Communications 57, no. 73 (2021): 9228–31. http://dx.doi.org/10.1039/d1cc03415d.
Повний текст джерелаJennings, M., and A. Hendrix. "Catalytic Carbocupration of Alkynoates." Synfacts 2010, no. 09 (August 23, 2010): 1032. http://dx.doi.org/10.1055/s-0030-1257956.
Повний текст джерелаLiu, Tong, Qiuping Ding, Qianshou Zong, and Guanyinsheng Qiu. "Radical 5-exo cyclization of alkynoates with 2-oxoacetic acids for synthesis of 3-acylcoumarins." Organic Chemistry Frontiers 2, no. 6 (2015): 670–73. http://dx.doi.org/10.1039/c5qo00029g.
Повний текст джерелаPiers, Edward, Timothy Wong, Philip D. Coish, and Christine Rogers. "A convenient procedure for the efficient preparation of alkyl (Z)-3-iodo-2-alkenoates." Canadian Journal of Chemistry 72, no. 8 (August 1, 1994): 1816–19. http://dx.doi.org/10.1139/v94-230.
Повний текст джерелаZeng, Piaopiao, Xiaoxiao Huang, Wei Tang, and Zhiwei Chen. "Copper-catalyzed cascade radical cyclization of alkynoates: construction of aryldifluoromethylated coumarins." Organic & Biomolecular Chemistry 19, no. 46 (2021): 10223–27. http://dx.doi.org/10.1039/d1ob01754c.
Повний текст джерелаQiu, Guanyinsheng, Tong Liu, and Qiuping Ding. "Tandem oxidative radical brominative addition of activated alkynes and spirocyclization: switchable synthesis of 3-bromocoumarins and 3-bromo spiro-[4,5] trienone." Organic Chemistry Frontiers 3, no. 4 (2016): 510–15. http://dx.doi.org/10.1039/c6qo00041j.
Повний текст джерелаNi, Shengyang, Jia Cao, Haibo Mei, Jianlin Han, Shuhua Li, and Yi Pan. "Sunlight-promoted cyclization versus decarboxylation in the reaction of alkynoates with N-iodosuccinimide: easy access to 3-iodocoumarins." Green Chemistry 18, no. 14 (2016): 3935–39. http://dx.doi.org/10.1039/c6gc01027j.
Повний текст джерелаPiers, Edward, Timothy Wong, and Keith A. Ellis. "Use of lithium (trimethylstannyl)(cyano)cuprate for the conversion of alkyl 2-alkynoates into alkyl (Z)- and (E)-3-trimethylstannyl-2-alkenoates." Canadian Journal of Chemistry 70, no. 7 (July 1, 1992): 2058–64. http://dx.doi.org/10.1139/v92-260.
Повний текст джерелаLuo, Zaigang, Xinxin Han, Chenfu Liu, Qiannan Liu, Rui Li, Peng Liu, and Xuemei Xu. "Catalyst-Free Synthesis of 1,4-Dihydroquinolines and Pyrrolo[1,2-a]quinolines via Intermolecular [4+2]/[3+2] Radical Cyclization of N-Methylanilines with Alkynoates." Synthesis 52, no. 07 (January 2, 2020): 1067–75. http://dx.doi.org/10.1055/s-0039-1691541.
Повний текст джерелаKolesinska, Beata. "P-Acylphosphonium salts and their vinyloges — application in synthesis." Open Chemistry 8, no. 6 (December 1, 2010): 1147–71. http://dx.doi.org/10.2478/s11532-010-0114-z.
Повний текст джерелаWakamatsu, Takamichi, Kazunori Nagao, Hirohisa Ohmiya, and Masaya Sawamura. "Copper-catalyzed stereoselective conjugate addition of alkylboranes to alkynoates." Beilstein Journal of Organic Chemistry 11 (December 4, 2015): 2444–50. http://dx.doi.org/10.3762/bjoc.11.265.
Повний текст джерелаLu, Xiyan, Yishu Du, and Cheng Lu. "Synthetic methodology using tertiary phosphines as nucleophilic catalysts." Pure and Applied Chemistry 77, no. 12 (January 1, 2005): 1985–90. http://dx.doi.org/10.1351/pac200577121985.
Повний текст джерелаMurayama, Hiroaki, Kazunori Nagao, Hirohisa Ohmiya, and Masaya Sawamura. "Phosphine-Catalyzed Vicinal Acylcyanation of Alkynoates." Organic Letters 18, no. 7 (March 24, 2016): 1706–9. http://dx.doi.org/10.1021/acs.orglett.6b00677.
Повний текст джерелаLu, Xiyan, and Qinghai Zhang. "Effect of ligands on the divalent palladium- catalyzed carbon-carbon coupling reactions. Highly enantioselective synthesis of optically active g-butyrolactones." Pure and Applied Chemistry 73, no. 2 (January 1, 2001): 247–50. http://dx.doi.org/10.1351/pac200173020247.
Повний текст джерелаHøyer, Thomas, Anders Kjær та Jens Lykkesfeldt. "A convenient synthesis of homochiral δ-alkylated α,β-unsaturated δ-lactones". Collection of Czechoslovak Chemical Communications 56, № 5 (1991): 1042–51. http://dx.doi.org/10.1135/cccc19911042.
Повний текст джерелаKim, Myung Hyun, Jaewon Choi, Kyoung Chul Ko, Kyoungil Cho, Ji Hoon Park, Sang Moon Lee, Hae Jin Kim, Yoon-Joo Ko, Jin Yong Lee, and Seung Uk Son. "Network-controlled unique reactivities of carbonyl groups in hollow and microporous organic polymer." Chemical Communications 54, no. 40 (2018): 5134–37. http://dx.doi.org/10.1039/c8cc02788a.
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